K231683
- 510(k) number
- K231683
- Device name
- inHEART Models
- Applicant
- Inheart, Sas FR
- Product code
- QIH — Automated Radiological Image Processing Software
- Decision date
- 2024-02-29
- Date received
- 2023-06-09
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K231683.pdf
Official FDA record: K231683
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.